Abstract
As part of concepts for chemical energy storage of excess chemical energy produced from renewable sources, we investigated the performance of CuO/ZnO catalysts supported on mesoporous carbon to convert CO2 hydrogenation to methanol. In this work, mesoporous carbon was used as the catalyst support for CuO-ZnO catalysts. Four catalysts with different precipitated precursors were synthesized and analyzed by N2-physisorption, X-ray diffraction (XRD), thermogravimetric analysis (TG-DTG), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The results show that catalyst CZ-in situ had the highest turnover frequency (TOF) (2.8 × 10−3 s−1) and methanol production rate (0.8 mmol g−1·h−1). The catalysts for co-precipitation of copper and zinc on carbon precursors are more active. Cu/ZnO domains that are accessible to the reactant gas are another reason for the catalysts being active. The Cu-ZnO interface is crucial to methanol catalyst activity.
Subject
Inorganic Chemistry,Condensed Matter Physics,General Materials Science,General Chemical Engineering
Cited by
2 articles.
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